HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → HCID 11052254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Product | HCID 11052254 | HCID 11052254 | 80% |
Reaction Steps
In a 50 mL-volumeric autoclave were added deaerated isopropanol (20 mL), 4-aminopyridine 47 mg (0.5 mmol) and (S)-epichlorohydrin (1.9 g, 20 mmol, >99% ee). Then to the mixture was added crystalline dicobaltoctacarbonyl complex (171 mg, 0.5 mmol). After covering the autoclave with a cap, carbon monoxide (1.5 MPa) was introduced therein and the mixture was reacted at 40° C. for 25 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-4-chloro-3-hydroxybutanoic acid isopropyl ester (2.7 g, 80%, >99% ee) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07256305B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-2afbe10ca0a8425f9499df0bd1aebf72 |
| Source note | uspto-grants-2007_08 |